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  • Genome-wide SNP genotyping study using pooled DNA to identify candidate markers mediating susceptibility to end-stage renal disease attributed to Type 1 diabetes
  • An association study of common variation at the MAPT locus with late-onset Alzheimer’s disease.
  • Targeted single nucleotide polymorphisms (SNP) discovery in a high polyploid plant species using 454 sequencing
  • The effect of smoking on MAOA promoter methylation in DNA prepared from lymphoblasts and whole blood
  • A systemativ association mapping on chromosome 6q in bipolar affective disorder – evidence for the melanin-concentrating-hormone-receptor-2 gene as a risk factor for bipolar-affective disorder
  • Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke.
  • Association between CYP2D6 polymorphisms and outcomes among women with early stage breast cancer treated with Tamoxifen
  • Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux
  • Programmed Death Ligand 1 (PD-L1) Gene Variants Contribute to Autoimmune Addison´s Disease and Graves´ Disease Susceptibility
  • Replication of Restless Legs Syndrome Loci in Three European Populations
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